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Comparison of the State Pharmacopoeia, XIII edition and the European Pharmacopoeia requirements for human plasma products

Abstract

Russian requirements for main products derived from human plasma used to be laid out in several nonintegrated monographs that have been recently included into the State Pharmacopoeia of the Russian Federation, XIII edition. The present article compares requirements for the quality of human plasma products that are contained in the State Pharmacopoeia, XIII edition and in the European Pharmacopoeia.

About the Authors

A. V. Karyakin
Hematology Research Center
Russian Federation


E. D. Skotselyas
Hematology Research Center
Russian Federation


References

1. Plasma for fractionation. FS 3.3.2.0001.15 (in Russian).

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5. The State Pharmacopoeia of the USSR. 11th ed. V. 1, 2. Moscow: Meditsina; 1987, 1990 (in Russian).

6. The State Pharmacopoeia of the Russian Federation. 12th ed. V. 1. Moscow: NCESMP; 2007 (in Russian).

7. European Pharmacopoeia. 8th edition. Strasbourg: EDQM; 2013.

8. Human Plasma for fractionation. Monograph Ph. Eur.8 0853 (in Russian).

9. Human Albumin solution. Monograph Ph. Eur.8 0255 (in Russian).

10. Human normal Immunoglobulin. Monograph Ph. Eur.8 0338 (in Russian).

11. Human normal Immunoglobulin for intravenous administration. Monograph Ph. Eur.8 0918 (in Russian).

12. Human von Willebrand factor. Monograph Ph. Eur.8 2298 (in Russian).

13. Human coagulation factor VII. Monograph Ph. Eur.8 1224 (in Russian).

14. Human coagulation factor VIII. Monograph Ph. Eur.8 0275 (in Russian).

15. Human coagulation factor IX. Monograph Ph. Eur.8 1223 (in Russian).


Review

For citations:


Karyakin A.V., Skotselyas E.D. Comparison of the State Pharmacopoeia, XIII edition and the European Pharmacopoeia requirements for human plasma products. The Bulletin of the Scientific Centre for Expert Evaluation of Medicinal Products. 2016;(2):50-52. (In Russ.)

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ISSN 3034-3062 (Print)
ISSN 3034-3453 (Online)